Aurevia

Aurevia was formed in 2025 when Scandinavian CRO, QAdvis, Artimed, Clinical Consulting, Kasve, Labquality, and P.R.I.S.M.A. CRO merged.

Expert consulting services in clinical research and medtech regulatory compliance

Aurevia offers consulting services within medtech regulatory compliance, as well as clinical research CRO services supporting pharmaceuticals, ATMPs, biologics, medical devices, and in vitro diagnostic devices. Our services for the healthcare, pharmaceutical, and medical technology sectors cover quality assurance, regulatory affairs, clinical studies, training, and more. 

With teams in the Nordics, Germany and Poland, we are highly skilled experts that support medical device and in vitro diagnostic (IVD) manufacturers, pharmaceutical companies, and academia throughout their product development. Together, we to pave the way for safer, more effective patient care worldwide.